Reappraisal of Frequency of Common Cystic Fibrosis Transmembrane Conductance Regulator Gene Mutations in Iranian Cystic Fibrosis Patients

BACKGROUND: Cystic Fibrosis (CF) is a life-threatening recessive genetic disorder resulting from mutations in the gene encoding the fibrosis transmembrane conductance regulator protein (CFTR). The CF clinical phenotype shows wide variation ranging from severe disease in early childhood in those homo...

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Bibliografske podrobnosti
izdano v:Tanaffos
Main Authors: Khalilzadeh, Soheila, Hassanzad, Maryam, PourAbdollah Toutkaboni, Mihan, Tashayoie Nejad, Sabereh, Sheikholeslami, Fatemeh-Maryam, Velayati, Ali Akbar
Format: Artigo
Jezik:Inglês
Izdano: National Research Institute of Tuberculosis and Lung Disease 2018
Teme:
Original Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC6320558/
https://ncbi.nlm.nih.gov/pubmed/30627177
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